The NovaSeq 6000 System unleashes a new era in sequencing with groundbreaking innovations, providing users with the throughput, speed, and flexibility to complete projects faster and more economically than ever before. Leveraging proven Illumina next-generation sequencing (NGS) technology, multiple flow cell types, two library loading workflows, and various read length combinations, the NovaSeq 6000 System enables effective throughput scaling to suit virtually any study needs.
The NovaSeq 6000 System unleashes a new era in sequencing with groundbreaking innovations, providing users with the throughput, speed, and flexibility to complete projects faster and more economically than ever before. Leveraging proven Illumina next-generation sequencing (NGS) technology, multiple flow cell types, two library loading workflows, and various read length combinations, the NovaSeq 6000 System enables effective throughput scaling to suit virtually any study needs. Applications requiring large amounts of data, such as human whole- genome sequencing (WGS), ultradeep exome sequencing, and tumor–normal profiling can now be completed in a more cost effective manner.
Features
2-color SBS chemistry.
Patterned Flowcell/ExAmp.
Two independent Flowcells.
Run time: 13-44 hrs.
Introduced in 2017.
Benefits
Human/Non-Human genome sequencing.
TruSightTM Oncology 500 Portfolio for CGP.
Whole Exomes sequencing.
RNA sequencing.
COVIDSeqTM Test (RUO).
Methyl sequencing.
Metagenomic profiling.
Targeted regions/large panel.
Single Cell applications.
Spatial transcriptome.
The NovaSeq 6000 System offers tremendous flexibility in sequencing options, supporting an extensive output range. Users can mix and match between four flow cell types (SP, S1, S2, or S4), run one or two flow cells at a time, and choose between multiple read lengths to easily adjust output and sample throughput for each sequencing run.
Common sequencing methods Whole-genome sequencing Illumina DNA PCR-Free Prep Illumina DNA Prep
Targeted resequencing
Illumina DNA Prep with Enrichment + Illumina Exome Panel Illumina RNA Prep with Enrichment + Illumina Exome Panel RNA sequencing
Illumina Stranded Total RNA Prep with Ribo-Zero Plus Illumina Stranded mRNA Library Prep
Epigenetic sequencing TruSeq Methyl Capture EPIC Unique dual indexing
IDT for Illumina DNA/RNA UD Indexes, Tagmentation (384 indexes across Sets A-D)
Large Whole-Genome Sequencing (human, plant, animal)
Small Whole-Genome Sequencing (microbe, virus)
Exome & Large Panel Sequencing (enrichment-based)
Targeted Gene Sequencing (amplicon-based, gene panel)
Single-Cell Profiling (scRNA-Seq, scDNA-Seq, oligo tagging assays)
Transcriptome Sequencing (total RNA-Seq, mRNA-Seq, gene expression profiling)
Chromatin Analysis (ATAC-Seq, ChIP-Seq)
Methylation Sequencing
Metagenomic Profiling (shotgun metagenomics, metatranscriptomics)
Cell-Free Sequencing & Liquid Biopsy Analysis
Run Time | ~13 – 38 hours (dual SP flow cells) ~13–25 hours (dual S1 flow cells) ~16–36 hours (dual S2 flow cells) ~44 hours (dual S4 flow cells) |
Maximum Output | 6000 Gb |
Maximum Reads Per Run | 20 billion |
Maximum Read Length | 2 x 250** |
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